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盐酸鲁拉西酮固体分散体的制备、表征及体外溶出行为研究 被引量:1

Preparation and Characterization of Lurasidone Hydrochloride Solid Dispersion and Study on the in vitro Dissolution Behavior
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摘要 目的:制备盐酸鲁拉西酮固体分散体,提高其溶出度。方法:选用聚维酮K30为载体,以溶剂法制备不同药载比(1:0.5、1:1、1:2)的盐酸鲁拉西酮固体分散体。比较3种盐酸鲁拉西酮固体分散体与物理混合物(盐酸鲁拉西酮-聚维酮K30)、原研制剂的体外溶出度;采用X射线粉末衍射法对盐酸鲁拉西酮原料药、聚维酮K30与外加辅料、物理混合物(1:2)与外加辅料、盐酸鲁拉西酮固体分散体(1:2)与外加辅料的晶体结构进行分析。结果:药载比1:0.5、1:1、1:2的盐酸鲁拉西酮固体分散体溶出速率较物理混合物有显著提高,且载体比例越大,固体分散体溶出越快;药载比为1:2的盐酸鲁拉西酮固体分散体与原研制剂20 min时体外溶出度分别为101.2%、100.2%。X射线粉末衍射结果显示,物理混合物中存在盐酸鲁拉西酮和辅料的特征吸收峰;盐酸鲁拉西酮固体分散体中的盐酸鲁拉西酮特征吸收峰基本消失,辅料特征吸收峰仍存在。结论:以药载比1:2制得的盐酸鲁拉西酮固体分散体与原研制剂体外溶出行为相似,且其中盐酸鲁拉西酮以无定形存在。 OBJECTIVE:To prepare the lurasidone hydrochloride solid dispersion,and improve its dissolution rate. METHODS:Taking povidone K30 as the carrier,solvent method was used to prepare the lurasidone hydrochloride solid dispersion with different drug-load ratios(1:0.5,1:1,1:2). The in vitro dissolution rates of 3 kinds of lurasidone hydrochloride solid dispersion with physical mixture(lurasidone hydrochloride-povidone K30)and original preparation were compared. X-ray powder diffraction method was adopted to analyze the crystal structures of raw material of lurasidone hydrochloride,povidone K30 and accessories,physical mixture(1:2)and accessories,and lurasidone hydrochloride solid dispersion(1:2)and accessories. RESULTS:Compared with physical mixture,the dissolution rate of lurasidone hydrochloride solid dispersion with drug-load ratios of 1:0.5,1:1,1:2 was significantly improved,and the dissolution rate of solid dispersion was increased as the increase of the carrier ratio. The in vitro dissolution rates of lurasidone hydrochloride solid dispersion with drug-load ratio of 1:2 and original preparation were respectively 101.2% and 100.2% in 20 min. X-ray powder diffraction showed,there were characteristic absorption peaks of lurasidone hydrochloride and accessories in physical mixture;the characteristic absorption peak of lurasidone hydrochloride in solid dispersion disappeared basically,and the characteristic absorption peak of accessories still existed. CONCLUSIONS:The in vitro dissolution of lurasidone hydrochloride solid dispersion with drug-load ratio of 1:2 is similar to original preparation,and lurasidone hydrochloride exists in the solid dispersion as amorphous form.
出处 《中国药房》 CAS 北大核心 2017年第34期4876-4878,共3页 China Pharmacy
关键词 盐酸鲁拉西酮 固体分散体 聚维酮K30 溶出度 Lurasidone hydrochloride Solid dispersion Povidone K30 Dissolution rate
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